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Allele specific chromatin signals, 3D interactions, and motif predictions for immune and B cell related diseases
Uppsala Univ, Dept Immunol Genet & Pathol, Sci Life Lab, Uppsala, Sweden..
Uppsala Univ, Dept Cell & Mol Biol Computat Biol & Bioinformat, Uppsala, Sweden..
Uppsala Univ, Dept Cell & Mol Biol Computat Biol & Bioinformat, Uppsala, Sweden..
Martin Luther Univ Halle Wittenberg, Inst Comp Sci, Halle, Germany..
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2019 (engelsk)Inngår i: Scientific Reports, ISSN 2045-2322, E-ISSN 2045-2322, Vol. 9, artikkel-id 2695Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Several Genome Wide Association Studies (GWAS) have reported variants associated to immune diseases. However, the identified variants are rarely the drivers of the associations and the molecular mechanisms behind the genetic contributions remain poorly understood. ChIP-seq data for TFs and histone modifications provide snapshots of protein-DNA interactions allowing the identification of heterozygous SNPs showing significant allele specific signals (AS-SNPs). AS-SNPs can change a TF binding site resulting in altered gene regulation and are primary candidates to explain associations observed in GWAS and expression studies. We identified 17,293 unique AS-SNPs across 7 lymphoblastoid cell lines. In this set of cell lines we interrogated 85% of common genetic variants in the population for potential regulatory effect and we identified 237 AS-SNPs associated to immune GWAS traits and 714 to gene expression in B cells. To elucidate possible regulatory mechanisms we integrated long-range 3D interactions data to identify putative target genes and motif predictions to identify TFs whose binding may be affected by AS-SNPs yielding a collection of 173 AS-SNPs associated to gene expression and 60 to B cell related traits. We present a systems strategy to find functional gene regulatory variants, the TFs that bind differentially between alleles and novel strategies to detect the regulated genes.

sted, utgiver, år, opplag, sider
NATURE PUBLISHING GROUP , 2019. Vol. 9, artikkel-id 2695
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URN: urn:nbn:se:kth:diva-246259DOI: 10.1038/s41598-019-39633-0ISI: 000459571100059PubMedID: 30804403Scopus ID: 2-s2.0-85062099213OAI: oai:DiVA.org:kth-246259DiVA, id: diva2:1299514
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QC 20190327

Tilgjengelig fra: 2019-03-27 Laget: 2019-03-27 Sist oppdatert: 2019-03-27bibliografisk kontrollert

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